Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/96170
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorChan, CMen_US
dc.creatorXing, Qen_US
dc.creatorChow, YCen_US
dc.creatorHung, SFen_US
dc.creatorYu, WYen_US
dc.date.accessioned2022-11-11T07:56:50Z-
dc.date.available2022-11-11T07:56:50Z-
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/10397/96170-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2019 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.9b03020.en_US
dc.titlePhotoredox decarboxylative C(sp³)-N coupling of α-diazoacetates with alkyl N-hydroxyphthalimide esters for diversified synthesis of functionalized N-alkyl hydrazonesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage8037en_US
dc.identifier.epage8043en_US
dc.identifier.volume21en_US
dc.identifier.issue19en_US
dc.identifier.doi10.1021/acs.orglett.9b03020en_US
dcterms.abstractHerein we report a metal-free photocatalytic coupling reaction for the synthesis of structurally and functionally diverse N-alkyl hydrazones from α-diazoacetates and N-alkyl hydroxyphthalimide esters. By employing Rose Bengal as a photocatalyst with yellow LEDs irradiation, over 60 N-alkyl hydrazones were synthesized. Fluorescence quenching analysis and deuterium incorporation experiments reveal that Hantzsch ester serves as both an electron donor and proton source for the reaction. This strategy offers a simple retrosynthetic disconnection for conventionally inaccessible C(sp³)-rich N-alkyl hydrazones.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOrganic letters, 4 Oct. 2019, v. 21, no. 19, p. 8037-8043en_US
dcterms.isPartOfOrganic lettersen_US
dcterms.issued2019-10-04-
dc.identifier.scopus2-s2.0-85072921786-
dc.identifier.pmid31524416-
dc.identifier.eissn1523-7052en_US
dc.description.validate202211 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberRGC-B3-0032, ABCT-0352-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe State Key Laboratory for Chemical Biology and Drug Discoveryen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS22434798-
Appears in Collections:Journal/Magazine Article
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